"61786-228-02" National Drug Code (NDC)

Famotidine 30 TABLET in 1 BLISTER PACK (61786-228-02)
(REMEDYREPACK INC.)

NDC Code61786-228-02
Package Description30 TABLET in 1 BLISTER PACK (61786-228-02)
Product NDC61786-228
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET
UsageORAL
Start Marketing Date20151026
Marketing Category NameANDA
Application NumberANDA075805
ManufacturerREMEDYREPACK INC.
Substance NameFAMOTIDINE
Strength40
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

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